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Home > Encyclopedia > Propanoic acid, 2-hydroxy-, compd. with 1-methyl-N-phenyl-N-(phenylmethyl)-4-piperidinamine (1:1)

Propanoic acid, 2-hydroxy-, compd. with 1-methyl-N-phenyl-N-(phenylmethyl)-4-piperidinamine (1:1)

Propanoic acid, 2-hydroxy-, compd. with 1-methyl-N-phenyl-N-(phenylmethyl)-4-piperidinamine (1:1) structure

Propanoic acid, 2-hydroxy-, compd. with 1-methyl-N-phenyl-N-(phenylmethyl)-4-piperidinamine (1:1) 

structure
  • CAS No:

    61670-09-5

  • Formula:

    C19H24N2.C3H6O3

  • Chemical Name:

    Propanoic acid, 2-hydroxy-, compd. with 1-methyl-N-phenyl-N-(phenylmethyl)-4-piperidinamine (1:1)

  • Synonyms:

    Propanoic acid,2-hydroxy-,compd. with 1-methyl-N-phenyl-N-(phenylmethyl)-4-piperidinamine (1:1);Piperidine,4-(N-benzylanilino)-1-methyl-,lactate;4-Piperidinamine,1-methyl-N-phenyl-N-(phenylmethyl)-,mono(2-hydroxypropanoate);Bamipine lactate

Propanoic acid, 2-hydroxy-, compd. with 1-methyl-N-phenyl-N-(phenylmethyl)-4-piperidinamine (1:1) Basic Attributes

370.48500

370.22564282

262-887-2

Characteristics

64.01000

3.17710

1.071g/cm3

412ºC

184.6ºC

Safety Information

|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P301+P312, P330, and P501|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

Drug Information

Drugs that bind to but do not activate histamine receptors, thereby blocking the actions of histamine or histamine agonists. Classical antihistaminics block the histamine H1 receptors only. (See all compounds classified as Histamine Antagonists.)

bamipine

Computed Properties

Molecular Weight:370.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:370.22564282
Monoisotopic Mass:370.22564282
Topological Polar Surface Area:64
Heavy Atom Count:27
Complexity:343
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

Guide of Propanoic acid, 2-hydroxy-, compd. with 1-methyl-N-phenyl-N-(phenylmethyl)-4-piperidinamine (1:1)

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